http://rdf.ncbi.nlm.nih.gov/pubchem/patent/TW-200815435-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c76ecadad74a1a35270b3e3a34d60f37
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P25-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2007-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_505ef7eed1ceb1ba67f11ce2ba9ac1ab
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3bd798693532b820ecb9dfb2eb106000
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7661113ba9dc2429a99a0f25b8dddcc0
publicationDate 2008-04-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber TW-200815435-A
titleOfInvention Process for making a tetrahydro-pyridoazepin-8-one related compound
abstract The present invention relates to a method of preparing 2-{4-[4-(7-fluoro-naphthalen-1-yl)-piperazin-1-yl]-butoxy}-5,6,7,9-tetrahydro-1,7,9-triaza-benzocyclohepten-8-one. The method comprises reacting 1-(7-fluoro-naphthalen-1-yl)-piperazine hydrochloride with a compound of formula (II), wherein L in formula (II) is a leaving group.
priorityDate 2006-03-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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